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Congenital cytomegalovirus pneumonia presents as pleural effusion in infancy
Nikhil Rajvanshi1, Taruna Yadav2, Prawin Kumar3
1Pediatrics, AIIMS Jodhpur, Jodhpur, Rajasthan, India.
Insights
Congenital Cytomegalovirus (CMV) infection can cause severe respiratory distress in newborns. Prompt diagnosis and treatment are crucial to prevent long-term complications like hearing loss and organ damage.
Area of Science:
- Neonatology
- Pediatric Infectious Diseases
- Congenital Infections
Background:
- Cytomegalovirus (CMV) infection is a common congenital infection.
- Congenital CMV can lead to significant neonatal morbidity.
- Early recognition is vital for managing potential complications.
Purpose of the Study:
- To highlight a case of congenital CMV presenting as neonatal pneumonitis.
- To emphasize the importance of early diagnosis and intervention.
Main Methods:
- Case presentation of an infant with respiratory distress since birth.
- Clinical examination, chest radiography, and contrast-enhanced CT of the thorax.
- Laboratory evaluation including CMV IgM antibodies and urinary CMV PCR.
- Audiological assessment for hearing loss.
Main Results:
- Infant presented with respiratory distress, bilateral pleural effusion, malnutrition, and microcephaly.
- Radiographic findings included diffuse haziness and interstitial pattern.
- CT revealed ground glass opacities, peribronchial thickening, and atelectasis.
- Diagnosis confirmed by positive CMV IgM and high viral load in urine.
- Bilateral moderate hearing loss was identified.
Conclusions:
- Congenital Cytomegalovirus can manifest as severe neonatal pneumonitis.
- Early diagnosis through clinical and laboratory evaluation is critical.
- Timely treatment can prevent permanent end-organ damage, including hearing loss.
Abstract:
Cytomegalovirus (CMV) infection is one of the most common congenital infections. We present a case of an infant who presented with respiratory distress since birth with a normal antenatal history. The infant had bilateral pleural effusion. He was malnourished with a small head. Chest auscultation revealed bilateral diffuse crepitation. The chest radiograph showed diffuse haziness with the interstitial pattern. Contrast-enhanced CT of the thorax showed diffuse areas of ground glass opacities with peribronchial thickening and patchy atelectasis in bilateral lower lobes. Detailed evaluation showed positive IgM CMV antibodies with >1000 copies/mL of CMV on urinary PCR. Hearing evaluation revealed bilateral moderate hearing loss.This case emphasises that CMV may present as pneumonitis at birth. Early diagnosis and treatment are of paramount importance in such cases, as it can prevent permanent end-organ damage.
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